Henry Schein 5700733Recalls & reported problems
Henry Schein, Inc. · 21G Safety Butterfly Blood Collection Needle · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10304040063627), received between May 16, 2025 and Jun 24, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Dull, Blunt2
- Complete Blockage1
Patient problems
- Pain3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 24, 2025Dull, Blunt; Dull, Blunt
THE CUSTOMER REPORTS THAT WHILE THEY WERE DRAWING BLOOD, THEY HAD A DOZEN PATIENTS THAT WERE COMPLAINING THAT THE NEEDLES HURT AS THEY WERE DULL. THEY HAVE USED THESE BEFORE. NO MEDICAL ATTENTION REQUIRED FOR ANY OF THE PATIENTS.
Patient problems: Pain
MAUDE report 22318544 ↗MalfunctionMay 16, 2025Complete Blockage; Complete Blockage
CUSTOMER REPORTED: THE CUSTOMER STATED THAT IT DOESN'T LET THE IV FLOW AND DOESN'T EXTRACT BLOOD - THEY SAID IT ALSO CAUSES PAIN TO THEIR PATIENTS.
Patient problems: Pain
MAUDE report 22035586 ↗MalfunctionMay 16, 2025Dull, Blunt; Dull, Blunt
CUSTOMER REPORTED: THE CUSTOMER ADVISED THAT THE NEEDLES ARE DULL AND THE PATIENTS ARE REPORTING THAT THEY ARE PAINFUL. "
Patient problems: Pain
MAUDE report 22035574 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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